Díaz-Gómez Dalia G, Galindo-Murillo Rodrigo, Cortés-Guzmán Fernando
Instituto de Quimica, Universidad Nacional Autonoma de Mexico, Av. Universidad 3000, Col. Copilco Bajo, 4510, Mexico, Mexico.
Medicinal Chemistry, University of Utah, 20 South 900 East, Salt Lake City, UT, 84047, USA.
Chemphyschem. 2017 Jul 19;18(14):1909-1915. doi: 10.1002/cphc.201700260. Epub 2017 May 29.
Molecular recognition between ligands and nucleic acids plays a key role in therapeutic activity. Some molecules interact with DNA in a nonbonded manner through intercalation or through the DNA grooves. The recognition of minor-groove binders is attributed to a set of hydrogen-bonding interactions between the binders and the hydrogen-bond-acceptor groups on the groove floor and walls. It is commonly considered that interactions with the sugar groups of the DNA backbone are insignificant and do not contribute to the binding affinity or the specificity. However, our group has found that the deoxyribose rings have a central function in the recognition and the intercalation of metal complexes into DNA. Herein, we determined the specific interactions between the binder CGP 40215A and the minor-groove atoms, based on the local properties of electron density. We found that specific interactions between the deoxyribose moiety within the backbone of DNA and the binder are essential for molecular recognition, and they are responsible for one third of the interaction energy.
配体与核酸之间的分子识别在治疗活性中起着关键作用。一些分子通过嵌入或通过DNA沟槽以非键合方式与DNA相互作用。对小沟结合剂的识别归因于结合剂与沟底和沟壁上的氢键受体基团之间的一组氢键相互作用。通常认为,与DNA主链糖基的相互作用微不足道,对结合亲和力或特异性没有贡献。然而,我们小组发现脱氧核糖环在金属配合物识别以及插入DNA过程中具有核心作用。在此,我们基于电子密度的局部性质确定了结合剂CGP 40215A与小沟原子之间的特定相互作用。我们发现,DNA主链内的脱氧核糖部分与结合剂之间的特定相互作用对于分子识别至关重要,它们占相互作用能的三分之一。